Results 31 to 40 of about 450,356 (259)

Genome-wide association studies in psychiatry: Current perspectives

European Psychiatry, 2021
Body Genome-wide Association Studies in Psychiatry - Current Perspectives Last decade was exciting time for human genetic studies. Genome-wide association studies (GWASs), used to examine the association of genotyped variants across the entire genome and
D. Smajlagic, T. Zayats, M. Bekkehus, S. Le Hellard   +3 more
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Clade distillation for genome-wide association studies. [PDF]

Genetics
Abstract Testing inferred haplotype genealogies for association with phenotypes has been a longstanding goal in human genetics with several underlying challenges. A key advantage of these methods is the potential to detect association signals caused by allelic heterogeneity — when multiple causal variants modulate a phenotype — in both ...
Christ R, Wang X, Aslett LJM, Steinsaltz D, Hall I.   +4 more
europepmc   +3 more sources

Genome-Wide Association Study of Opioid Cessation [PDF]

Journal of Clinical Medicine, 2020
The United States is experiencing an epidemic of opioid use disorder (OUD) and overdose-related deaths. However, the genetic basis for the ability to discontinue opioid use has not been investigated. We performed a genome-wide association study (GWAS) of opioid cessation (defined as abstinence from illicit opioids for >1 year or <6 months before ...
Jiayi W. Cox, Richard M. Sherva, Kathryn L. Lunetta, Emma C. Johnson, Nicholas G. Martin, Louisa Degenhardt, Arpana Agrawal, Elliot C. Nelson, Henry R. Kranzler, Joel Gelernter, Lindsay A. Farrer   +10 more
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Simulating variance heterogeneity in quantitative genome wide association studies

BMC Bioinformatics, 2018
Background Analyzing Variance heterogeneity in genome wide association studies (vGWAS) is an emerging approach for detecting genetic loci involved in gene-gene and gene-environment interactions.
Ahmad Al Kawam, Mustafa Alshawaqfeh, James J. Cai, Erchin Serpedin, Aniruddha Datta   +4 more
doaj   +1 more source

Status and prospects of genome‐wide association studies in plants

The Plant Genome, 2021
Genome‐wide association studies (GWAS) have developed into a powerful and ubiquitous tool for the investigation of complex traits. In large part, this was fueled by advances in genomic technology, enabling us to examine genome‐wide genetic variants ...
Laura Tibbs Cortes, Zhiwu Zhang, Jianming Yu   +2 more
doaj   +1 more source

Genome-wide association studies in mice [PDF]

Nature Reviews Genetics, 2012
Genome-wide association studies (GWASs) have transformed the field of human genetics and have led to the discovery of hundreds of genes that are implicated in human disease. The technological advances that drove this revolution are now poised to transform genetic studies in model organisms, including mice.
Flint, J, Eskin, E
openaire   +3 more sources

Genome-wide association studies: a primer [PDF]

Psychological Medicine, 2009
There have been nearly 400 genome-wide association studies (GWAS) published since 2005. The GWAS approach has been exceptionally successful in identifying common genetic variants that predispose to a variety of complex human diseases and biochemical and anthropometric traits. Although this approach is relatively new, there are many excellent reviews of
Corvin, A., Craddock, Nicholas John, Sullivan, P. F.   +2 more
openaire   +4 more sources

Genome-wide association study of long COVID

Nature Genetics, 2023
Abstract Infections can lead to persistent symptoms and diseases such as shingles after varicella zoster or rheumatic fever after streptococcal infections. Similarly, severe acute respiratory syndrome coronavirus 2 (SARS‑CoV‑2) infection can result in long coronavirus disease (COVID), typically manifesting as ...
Vilma Lammi, Tomoko Nakanishi, Samuel E. Jones, Shea J. Andrews, Juha Karjalainen, Beatriz Cortés, Heath E. O’Brien, Ana Ochoa-Guzman, Brian E. Fulton-Howard, Martin Broberg, Hele H. Haapaniemi, Masahiro Kanai, Matti Pirinen, Axel Schmidt, Ruth E. Mitchell, Abdou Mousas, Massimo Mangino, Alicia Huerta-Chagoya, Nasa Sinnott-Armstrong, Elizabeth T. Cirulli, Marc Vaudel, Alex S. F. Kwong, Amit K. Maiti, Minttu M. Marttila, Daniel C. Posner, Alexis A. Rodriguez, Chiara Batini, Francesca Minnai, Anna R. Dearman, C. A. Robert Warmerdam, Celia B. Sequeros, Thomas W. Winkler, Daniel M. Jordan, Raimonds Rešcenko, Lorenzo Miano, Jacqueline M. Lane, Ryan K. Chung, Beatriz Guillen-Guio, Olivia C. Leavy, Laura Carvajal-Silva, Kevin Aguilar-Valdés, Erika Frangione, Lindsay Guare, Ekaterina Vergasova, Eirini Marouli, Pasquale Striano, Ummu Afeera Zainulabid, Ashutosh Kumar, Hajar Fauzan Ahmad, Ryuya Edahiro, Shuhei Azekawa, Mari E. K. Niemi, Janick St-Cyr, Darin Adra, Madeleine Durand, David Bujold, Guillaume Bourque, Ariane Boisclair, Mylene Bertrand, Daniel Auld, Laetitia Laurent, Solomia Yanishevsky, G. Mark Lathrop, Fangyi Shi, Simon Rousseau, Jiannis Ragoussis, Danielle Perley, Vincent Mooser, David R. Morrison, Daniella Balla, Julia Heggemann, Sonja Schultz, Pari Behzad, Markus M. Nöthen, Abigail Miller, Max C. Pensel, Carlo Maj, Kelly Cho, Tianxi Cai, Sudha K. Iyengar, Carlos A. Aguilar Salinas, Seung Hyuk T. Lee, Hortensia Moreno-Macias, Päivi Pajukanta, Michelle Duran-Gomez, Lill Trogstad, Daniel J. Rader, Marylyn D. Ritchie, Anurag Verma, Colleen M. Kripke, Sergi Papiol, Jens Wiltfang, Jochen Schneider, Thomas G. Schulze, Christof Winter, Ewa Wallin, Robert Frithiof, Fanny Senner, Christoph D. Spinner, Ulrike Protzer, Mattia Cordioli, Nikola S. Mueller, Andreas Dinkel, Janos L. Kalman, Tomislav Maricic, Kristina Adorjan, Miklos Lipcsey, Lisa Fricke, Ing-Marie Larsson, Urs Heilbronner, Monika Budde, Johanna Erber, Nicholas R. Harvey, Vince Forgetta, Benedict Hignell, Yolanda Espinosa-Parrilla, Juan M. Saez Hidalgo, Estefania Nova-Lamperti, Scarlett Gutiérrez-Richards, Gerardo Donoso, Leslie C. Cerpa, Cesar A. Echeverria, Camilo Cabrera, Pamela Bocchieri, Macarena Fuentes-Guajardo, Christian A. Muñoz, Karen Y. Oróstica, Alvaro Figueroa, Lissette G. Guajardo, Iskra A. Signore, Virginia A. Monardes-Ramírez, Eduardo A. Tobar-Calfucoy, Luis A. Quiñones, Cristian E. Yáñez, Daniela Zapata-Contreras, Paula Zuñiga-Pacheco, Romina Quiroga, Matías F. Martínez, Teresa A. Alarcon, Andrea X. Silva, Carolina S. Selman, Sergio Sanhueza, Rocío Retamales-Ortega, Tamara V. Arévalo, Eduardo Lamoza, Héctor Valenzuela-Jorquera, Maria Sophia Donaire, Sannidhi Sarvadhavabhatla, Sisse R. Ostrowski, Søren Brunak, David Westergaard, Bjarke Feenstra, Anne Sofie B. Mortensen, Anna L. Guyatt, Rafael de Cid, Susana Iraola-Guzmán, Gemma Moncunill, Alba Blasco, Judith Garcia-Aymerich, Natalia Blay, Carlota Dobaño, Anna Carreras, Xavier Farré, Manolis Kogevinas, Gemma Castaño-Vinyals, Simone Furini, Chiara Fallerini, Kristina Zguro, Margherita Baldassarri, Francesca Colombo, Thompson Hannah, Anna Ilinskaya, Michil Trofimov, Layal Shaheen, Nikolay Plotnikov, Anna Kim, Dmitrii Kharitonov, Valery Ilinsky, Alexei Kamelin, Francisco Tanudjaja, Efren Sandoval, Nicole L. Washington, Simon White, Iva Neveux, Shaun Dabe, Alexandre Bolze, Kelly M. Schiabor Barrett, Eirini Christaki, Haralampos Milionis, Ioanna Tzoulaki, Angelos Liontos, Evangelos Evangelou, Evangelia Ntzani, Rasoul Aliannejad, Vahideh Zarei, Nastaran Soltani, Bahareh Sharififard, Hengameh Ansari Tadi, Ali Amirsavadkouhi, Ho NamKoong, Olga Vishnyakova, Jakob M. Cherry, Marco Mantero, Alessandra Bandera, Francesco Bruno Arturo Blasi, Christian Erikstrup, Ole B. V. Pedersen, Joseph J. Grzymski, Makoto Ishii, Yukinori Okada, Noam D. Beckmann, Meena Kumari, Ralf Wagner, Iris M. Heid, Catherine John, Patrick J. Short, Per Magnus, Laura Ansone, Luca V. C. Valenti, Sulggi A. Lee, Louise V. Wain, Ricardo A. Verdugo, Karina Banasik, Frank Geller, Lude H. Franke, Alexander Rakitko, Emma L. Duncan, Alessandra Renieri, Konstantinos K. Tsilidis, Rafael de Cid, Ahmadreza Niavarani, Erik Abner, Teresa Tusié-Luna, Shefali S. Verma, George Davey Smith, Nicholas J. Timpson, Ravi K. Madduri, Andrea Ganna, Eva C. Schulte, J. Brent Richards, Kerstin U. Ludwig, Michael Marks-Hultström, Hugo Zeberg, Hanna M. Ollila   +243 more
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Genome-wide association study of Tourette's syndrome [PDF]

Molecular Psychiatry, 2012
Tourette's syndrome (TS) is a developmental disorder that has one of the highest familial recurrence rates among neuropsychiatric diseases with complex inheritance. However, the identification of definitive TS susceptibility genes remains elusive. Here, we report the first genome-wide association study (GWAS) of TS in 1285 cases and 4964 ancestry ...
Scharf, JM, Yu, D, Mathews, CA, Neale, BM, Stewart, SE, Fagerness, JA, Evans, P, Gamazon, E, Edlund, CK, Service, SK, Tikhomirov, A, Osiecki, L, Illmann, C, Pluzhnikov, A, Konkashbaev, A, Davis, LK, Han, B, Crane, J, Moorjani, P, Crenshaw, AT, Parkin, MA, Reus, VI, Lowe, TL, Rangel-Lugo, M, Chouinard, S, Dion, Y, Girard, S, Cath, DC, Smit, JH, King, RA, Fernandez, TV, Leckman, JF, Kidd, KK, Kidd, JR, Pakstis, AJ, State, MW, Herrera, LD, Romero, R, Fournier, E, Sandor, P, Barr, CL, Phan, N, Gross-Tsur, V, Benarroch, F, Pollak, Y, Budman, CL, Bruun, RD, Erenberg, G, Naarden, AL, Lee, PC, Weiss, N, Kremeyer, B, Berrío, GB, Campbell, DD, Cardona Silgado, JC, Ochoa, WC, Mesa Restrepo, SC, Muller, H, Valencia Duarte, AV, Lyon, GJ, Leppert, M, Morgan, J, Weiss, R, Grados, MA, Anderson, K, Davarya, S, Singer, H, Walkup, J, Jankovic, J, Tischfield, JA, Heiman, GA, Gilbert, DL, Hoekstra, PJ, Robertson, MM, Kurlan, R, Liu, C, Gibbs, JR, Singleton, A, North American Brain Expression Consortium, Hardy, J, UK Human Brain Expression Database, Strengman, E, Ophoff, RA, Wagner, M, Moessner, R, Mirel, DB, Posthuma, D, Sabatti, C, Eskin, E, Conti, DV, Knowles, JA, Ruiz-Linares, A, Rouleau, GA, Purcell, S, Heutink, P, Oostra, BA, McMahon, WM, Freimer, NB, Cox, NJ, Pauls, DL   +99 more
openaire   +10 more sources

Genome Wide Association Studies Using Multiple-lactation Breeding Value in Holsteins [PDF]

Asian-Australasian Journal of Animal Sciences, 2015
A genome wide association study was conducted using estimated breeding value (EBV) for milk production traits from 1st to 4th lactation. Significant single nucleotide polymorphism (SNP) markers were selected for each trait and the differences were ...
Kwang-Hyun Cho, Jae-Don Oh, Hee-bal Kim, Kyung-Do Park, Joon-Ho Lee   +4 more
doaj   +1 more source